MIR3059[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	LOC130008916, LOC130008917 +4836 more	Copy number gain	See cases	GPathogenic
Select item 155032	GRCh38/hg38 12q21.1-22(chr12:73485697-92795805)x1	ACSS3, ALX1 +287 more	Copy number loss	See cases	GPathogenic
Select item 153857	GRCh38/hg38 12q21.32(chr12:86403298-87522344)x3	LOC105369879, LOC126861590 +4 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 151341	GRCh38/hg38 12q21.32(chr12:86429352-87327461)x1	LOC130008343, LOC130008344 +2 more	Copy number loss	See cases	GLikely benign
Select item 150577	GRCh38/hg38 12q21.32(chr12:86443917-87324781)x1	LOC130008343, LOC130008344 +2 more	Copy number loss	See cases	GUncertain significance
Select item 150338	GRCh38/hg38 12q21.32(chr12:86572479-86881491)x1	MGAT4C, MIR3059	Copy number loss	See cases	GLikely benign

ClinVar